Published in Am J Hum Genet on June 06, 2006
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Mutational mechanisms of Williams-Beuren syndrome deletions. Am J Hum Genet (2003) 3.76
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A susceptibility gene for late-onset idiopathic Parkinson's disease. Ann Neurol (2002) 1.92
Localization of a susceptibility gene for common forms of stroke to 5q12. Am J Hum Genet (2002) 1.67
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Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome. Hum Mol Genet (1995) 1.37
A genome-wide survey of segmental duplications that mediate common human genetic variation of chromosomal architecture. Hum Genomics (2004) 1.22
Linkage of essential hypertension to chromosome 18q. Hypertension (2002) 1.03
Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization. Am J Med Genet (1995) 0.98
Merging microsatellite data. J Comput Biol (2006) 0.88
Large recurrent microdeletions associated with schizophrenia. Nature (2008) 20.25
Fast model-based estimation of ancestry in unrelated individuals. Genome Res (2009) 15.63
Genome-wide association analysis by lasso penalized logistic regression. Bioinformatics (2009) 12.21
Common variants conferring risk of schizophrenia. Nature (2009) 10.37
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Nat Genet (2011) 7.98
Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet (2013) 7.44
Multiple common variants for celiac disease influencing immune gene expression. Nat Genet (2010) 6.90
Prioritizing GWAS results: A review of statistical methods and recommendations for their application. Am J Hum Genet (2010) 5.39
Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet (2002) 4.89
Disruption of the neurexin 1 gene is associated with schizophrenia. Hum Mol Genet (2008) 4.78
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat Genet (2009) 4.38
Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet (2012) 3.73
Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. PLoS Genet (2011) 3.65
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat Genet (2010) 3.55
The relationship of DNA methylation with age, gender and genotype in twins and healthy controls. PLoS One (2009) 3.41
Aging effects on DNA methylation modules in human brain and blood tissue. Genome Biol (2012) 3.05
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study. Lancet Neurol (2007) 2.80
Association screening of common and rare genetic variants by penalized regression. Bioinformatics (2010) 2.67
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. Nat Genet (2007) 2.63
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. Nat Genet (2010) 2.61
Recurrent CNVs disrupt three candidate genes in schizophrenia patients. Am J Hum Genet (2008) 2.61
A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. Nat Genet (2010) 2.56
Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen. Lancet Neurol (2008) 2.54
Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression. PLoS Genet (2012) 2.29
Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Hum Mol Genet (2011) 2.21
Penalized estimation of haplotype frequencies. Bioinformatics (2008) 2.19
Enhancements to the ADMIXTURE algorithm for individual ancestry estimation. BMC Bioinformatics (2011) 2.16
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biol Psychiatry (2010) 2.07
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. Proc Natl Acad Sci U S A (2009) 2.03
Wnt signaling and Dupuytren's disease. N Engl J Med (2011) 2.02
Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. Am J Psychiatry (2011) 1.94
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging Behav (2014) 1.90
Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. Nat Genet (2011) 1.88
A quasi-Newton acceleration for high-dimensional optimization algorithms. Stat Comput (2011) 1.80
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. PLoS Genet (2011) 1.80
Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients. BMC Genomics (2009) 1.72
Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects. BMC Genomics (2012) 1.70
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genet (2013) 1.68
European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene. Hum Mol Genet (2011) 1.58
Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration. Hum Mol Genet (2008) 1.46
A gene co-expression network in whole blood of schizophrenia patients is independent of antipsychotic-use and enriched for brain-expressed genes. PLoS One (2012) 1.45
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. Ann Neurol (2011) 1.45
Fine mapping of regulatory loci for mammalian gene expression using radiation hybrids. Nat Genet (2008) 1.41
Migraine: a complex genetic disorder. Lancet Neurol (2007) 1.39
MM Algorithms for Some Discrete Multivariate Distributions. J Comput Graph Stat (2010) 1.36
Gene networks associated with conditional fear in mice identified using a systems genetics approach. BMC Syst Biol (2011) 1.30
At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia. Biol Psychiatry (2011) 1.26
Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder. Schizophr Res (2012) 1.24
Gene-network analysis identifies susceptibility genes related to glycobiology in autism. PLoS One (2009) 1.23
Association testing in a linked region using large pedigrees. Am J Hum Genet (2005) 1.23
A genome-wide survey of segmental duplications that mediate common human genetic variation of chromosomal architecture. Hum Genomics (2004) 1.22
Is human blood a good surrogate for brain tissue in transcriptional studies? BMC Genomics (2010) 1.22
Linkage analysis without defined pedigrees. Genet Epidemiol (2011) 1.20
Strong correlation between meiotic crossovers and haplotype structure in a 2.5-Mb region on the long arm of chromosome 21. Genome Res (2005) 1.20
Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug-induced weight gain. Arch Gen Psychiatry (2012) 1.20
Genetic contributions to social impulsivity and aggressiveness in vervet monkeys. Biol Psychiatry (2004) 1.19
Genotype imputation via matrix completion. Genome Res (2012) 1.18
Stability selection for genome-wide association. Genet Epidemiol (2011) 1.18
Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients. Biol Psychiatry (2011) 1.18
Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes. Eur J Hum Genet (2012) 1.14
Analysis of genome-wide copy number variation in Irish and Dutch ALS populations. Hum Mol Genet (2008) 1.12
Graphics Processing Units and High-Dimensional Optimization. Stat Sci (2010) 1.10
Three ulcerative colitis susceptibility loci are associated with primary sclerosing cholangitis and indicate a role for IL2, REL, and CARD9. Hepatology (2011) 1.09
A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. Hum Mol Genet (2010) 1.08
FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands. Arch Neurol (2010) 1.08
A quantitative trait locus for variation in dopamine metabolism mapped in a primate model using reference sequences from related species. Proc Natl Acad Sci U S A (2007) 1.04
A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus). Mamm Genome (2007) 1.04
Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome. Am J Med Genet B Neuropsychiatr Genet (2009) 1.02
Paternal age and psychiatric disorders: findings from a Dutch population registry. Schizophr Res (2011) 1.01
Finding suitable phenotypes for genetic studies of schizophrenia: heritability and segregation analysis. Biol Psychiatry (2008) 1.01
Genetic studies of neuropsychiatric disorders in Costa Rica: a model for the use of isolated populations. Psychiatr Genet (2004) 1.01
RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION. Ann Appl Stat (2010) 1.01
The association of the alpha-5 subunit of the nicotinic acetylcholine receptor gene and the brain-derived neurotrophic factor gene with different aspects of smoking behavior. Psychiatr Genet (2012) 0.99
A common variant in DRD3 receptor is associated with autism spectrum disorder. Biol Psychiatry (2008) 0.98
A Path Algorithm for Constrained Estimation. J Comput Graph Stat (2013) 0.97
Current status and future prospects for epigenetic psychopharmacology. Epigenetics (2012) 0.96
Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. Biol Psychiatry (2012) 0.96
Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex. PLoS One (2010) 0.96
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. PLoS One (2012) 0.95
Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis. PLoS One (2012) 0.95
Codon and rate variation models in molecular phylogeny. Mol Biol Evol (2002) 0.94
A Poisson model for random multigraphs. Bioinformatics (2010) 0.94
Kraepelin was right: a latent class analysis of symptom dimensions in patients and controls. Schizophr Bull (2010) 0.94
Genetic overlap among intelligence and other candidate endophenotypes for schizophrenia. Biol Psychiatry (2008) 0.94
New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. Int J Epidemiol (2015) 0.93
Modeling maternal-offspring gene-gene interactions: the extended-MFG test. Genet Epidemiol (2010) 0.93
Vocabulon: a dictionary model approach for reconstruction and localization of transcription factor binding sites. Bioinformatics (2004) 0.93
Common genetic variations in CCK, leptin, and leptin receptor genes are associated with specific human eating patterns. Diabetes (2007) 0.92
A large genome scan for rare CNVs in amyotrophic lateral sclerosis. Hum Mol Genet (2010) 0.92
TCF4 (e2-2; ITF2): a schizophrenia-associated gene with pleiotropic effects on human disease. Am J Med Genet B Neuropsychiatr Genet (2012) 0.91
Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. BMC Genomics (2012) 0.91
Powerful allele sharing statistics for nonparametric linkage analysis. Hum Hered (2004) 0.91
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. Am J Psychiatry (2014) 0.90
Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder. Biol Psychiatry (2012) 0.89
No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet (2011) 0.89
Quantitative trait Loci association mapping by imputation of strain origins in multifounder crosses. Genetics (2011) 0.89
Prediction of serotonin transporter promoter polymorphism genotypes from single nucleotide polymorphism arrays using machine learning methods. Psychiatr Genet (2012) 0.89
Merging microsatellite data. J Comput Biol (2006) 0.88